Overview

IL-4(38-37)-PE38KDEL Immunotoxin in Treating Patients With Recurrent Malignant Astrocytoma

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: IL-4(38-37)-PE38KDEL immunotoxin may locate tumor cells and kill them without harming normal cells. This may be an effective treatment for recurrent malignant astrocytoma. PURPOSE: Phase I trial to study the effectiveness of IL-4(38-37)-PE38KDEL immunotoxin in treating patients who have recurrent malignant astrocytoma.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Barrett Cancer Center
Treatments:
Interleukin-4
Criteria
DISEASE CHARACTERISTICS: Histologically proven recurrent glioblastoma or anaplastic
astrocytoma Stereotactically accessible, enhancing mass no greater than 50 mL total volume
by MRI No significant mass effect Recent craniotomy allowed No anaplastic oligodendroglioma
No tumors of the brainstem, cerebellum, or both hemispheres No diffuse subependymal or CSF
disease If on stable or increasing dose of steroid, must have evidence of increasing
contrast enhancement by MRI or CT scan Prior external beam radiotherapy required

PATIENT CHARACTERISTICS: Age: Over 18 Performance status: Karnofsky 60-100% Life
expectancy: Not specified Hematopoietic: Absolute neutrophil count greater than 1500/mm3
Platelet count greater than 100,000/mm3 Hemoglobin greater than 9.5 g/dL Hepatic: Bilirubin
less than 2 mg/dL AST and ALT less than 2 times upper limit of normal (ULN) PT/PTT no
greater than ULN Renal: Creatinine less than 2 mg/dL Other: Not pregnant Negative pregnancy
test Fertile patients must use effective contraception No systemic diseases to cause
unacceptable anesthetic/operative risk No active infection requiring treatment No
unexplained febrile illness

PRIOR CONCURRENT THERAPY: Biologic therapy: No concurrent blood or platelet transfusions
Chemotherapy: At least 4 weeks since prior chemotherapy Endocrine therapy: See Disease
Characteristics Radiotherapy: See Disease Characteristics At least 4 weeks since prior
radiotherapy Surgery: See Disease Characteristics Medically able to undergo surgery Other:
No other concurrent investigational agents